FAM59A antibody (AA 151-250)

Catalog No. ABIN873242

Product Details anti-FAM59A Antibody

Target: FAM59A (Family with Sequence Similarity 59, Member A (FAM59A))

Binding Specificity: AA 151-250

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM59A antibody is un-conjugated

Application: ELISA, Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAM59A

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for FAM59A

Target: FAM59A (Family with Sequence Similarity 59, Member A (FAM59A))

Alternative Name: Fam59a (FAM59A Products)

Synonyms: C18orf11 antibody, FAM59A antibody, Gm944 antibody, C86169 antibody, Fam59a antibody, mKIAA4238 antibody, fam59a antibody, zgc:55634 antibody, GRB2 associated regulator of MAPK1 subtype 1 antibody, GRB2 associated, regulator of MAPK1 antibody, GAREM1 antibody, Garem1 antibody, garem antibody

Background:

Synonyms: FA59A_HUMAN, fam59a, Family with sequence similarity 59, member A, GAREM, Gm944, Protein FAM59A.

Background: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization.

Gene ID: 64762

Pathways: EGFR Signaling Pathway